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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Key value for chemical safety assessment

Genetic toxicity in vitro

Description of key information

Several in vitro assays (Ames tests, a chromosome aberration test, a HGPRT assay, 2 SCE assays and several UDS/DNA repair assays) are published. Additionally an in-vitro micronuleus test in chinese hamster V79 cells according to OECD TG 487 was conducted.
No in vivo assay is available.

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (positive)

Genetic toxicity in vivo

Description of key information

No in vivo assay is available.

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

In the Ames test, 1,4-dihydroxyanthraquinoe was positive (with the exception of those assays were only a limited number of S. typhimurium strains were used. 1,4-dihydroxyanthraquinone was also positive in the CA test and the in-vitro micronucleus test in Chinese hamster V79 cells.

In the HGPRT test and the UDS/DNA repair assays, 1,4-dihydroxyanthraquinone was negative, also in the genotoxicity assay in Saccharomyces cervesia. In the SCE assay, 1,4-dihydroxyanthraquinone revealed a weak (and dose independent) effect.

In 2 in vitro DNA binding assays a positive and a negative result was obtained (see section 7.9.3 specific investigations).




Justification for classification or non-classification

In the Ames tests, the chromosome aberration test and the in-vitro MNT a positive result was obtainded. In the HGPRT test and the UDS/DNA repair assays, 1,4-dihydroxyanthraquinone was negative, also in the genotoxicity assay in Saccharomyces cervesia. In the SCE assay, 1,4-dihydroxyanthraquinone revealed a weak (and dose independent) effect.

In 2 in vitro DNA binding assays a positive and a negative result was obtained (see section 7.9.3 specific investigations).

Overall, 1,4-dihydroxyanthraquinone was positive in several in-vitro assays, but no in-vivo studies are available. Based on the inconclusive results a classification according to CLP classification criteria (Regulation (EC) No 1272/2008) is not suitable, however due to the ambigouos results 1,4-dihydroxyanthraquinone is allocated to the medium hazard band.